15459-85-5 Usage
Uses
Used in Pharmaceutical Industry:
Lathosterone is used as a pharmaceutical compound for its potential therapeutic properties. It may be utilized in the development of drugs targeting specific medical conditions due to its unique chemical structure and steroidal nature.
Used in Chemical Research:
In the field of chemical research, Lathosterone can be used as a starting material or intermediate in the synthesis of other complex steroidal compounds. Its unique structure makes it a valuable tool for understanding the properties and functions of related molecules.
Used in Cosmetics Industry:
Lathosterone may also find applications in the cosmetics industry, where it could be used as an active ingredient in anti-aging or skin care products. Its steroidal nature may contribute to potential benefits for skin health and appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 15459-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,5 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15459-85:
(7*1)+(6*5)+(5*4)+(4*5)+(3*9)+(2*8)+(1*5)=125
125 % 10 = 5
So 15459-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h10,18-20,23-25H,6-9,11-17H2,1-5H3/t19-,20?,23-,24+,25+,26+,27-/m1/s1
15459-85-5Relevant articles and documents
LIGANDS FOR NEMATODE NUCLEAR RECEPTORS AND USES THEREOF
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Page/Page column 27, (2008/06/13)
Anti-nematode compounds, compositions, and methods for identifying such compounds are disclosed, where the compounds have the formula I: where Q, Q′, R1, R2, and n are defined herein.
Synthesis of a tritiated 3-dehydroecdysteroid putative precursor of ecdysteroid biosynthesis in Locusta migratoria
Dolle,Hetru,Roussel,Rousseau,Sobrio,Luu,Hoffmann
, p. 7067 - 7080 (2007/10/02)
We have synthesized a tritiated form of 14α-hydroxy-5β-cholest-7-ene-3,6-dione (5β-diketol) of high specific activity (1.74 TBq/mmol) from 7-dehydrocholesterol in seven steps with stereoselective introduction of the A/B cis ring junction as the key reaction. We have examined the ability of endocrine glands (prothoracic glands) of Locusta migratoria to use this molecule as a precursor of 3-dehydroecdysone and of ecdysone biosynthesis. A very efficient conversion of 5β-diketol to ecdysone and to 3-dehydroecdysone was monitored, which opens up new possibilities for the understanding of the role of 3-dehydro-compounds in ecdysteroid biosynthesis.
